Year: 2021 Source: Psychiatric Research and Clinical Practice. (2020). xx:0. Published online:21 December 2020. https://doi.org/10.1176/appi.prcp.20200029 SIEC No: 20210081

Objective
Digital monitoring technologies (e.g., smartphones and wearable devices) provide unprecedented opportunities to study potentially harmful behaviors such as suicide, violence, and alcohol/substance use in real‐time. The use of these new technologies has the potential to significantly advance the understanding, prediction, and prevention of these behaviors. However, such technologies also introduce myriad ethical and safety concerns, such as deciding when and how to intervene if a participant’s responses indicate elevated risk during the study?

Methods
We used a modified Delphi process to develop a consensus among a diverse panel of experts on the ethical and safety practices for conducting digital monitoring studies with those at risk for suicide and related behaviors. Twenty‐four experts including scientists, clinicians, ethicists, legal experts, and those with lived experience provided input into an iterative, multi‐stage survey, and discussion process.

Results
Consensus was reached on multiple aspects of such studies, including: inclusion criteria, informed consent elements, technical and safety procedures, data review practices during the study, responding to various levels of participant risk in real‐time, and data and safety monitoring.

Conclusions
This consensus statement provides guidance for researchers, funding agencies, and institutional review boards regarding expert views on current best practices for conducting digital monitoring studies with those at risk for suicide—with relevance to the study of a range of other potentially harmful behaviors (e.g., alcohol/substance use and violence). This statement also highlights areas in which more data are needed before consensus can be reached regarding best ethical and safety practices for digital monitoring studies.